000 | 00980 a2200277 4500 | ||
---|---|---|---|
005 | 20250513122037.0 | ||
264 | 0 | _c19970909 | |
008 | 199709s 0 0 eng d | ||
022 | _a0141-8955 | ||
024 | 7 |
_a10.1023/a:1005388218625 _2doi |
|
040 |
_aNLM _beng _cNLM |
||
100 | 1 | _aHarper, P S | |
245 | 0 | 0 |
_aTrinucleotide repeat disorders. _h[electronic resource] |
260 |
_bJournal of inherited metabolic disease _cJun 1997 |
||
300 |
_a122-4 p. _bdigital |
||
500 | _aPublication Type: Journal Article | ||
650 | 0 | 4 |
_aFragile X Syndrome _xgenetics |
650 | 0 | 4 | _aHumans |
650 | 0 | 4 |
_aHuntington Disease _xgenetics |
650 | 0 | 4 |
_aMetabolic Diseases _xgenetics |
650 | 0 | 4 |
_aMuscular Atrophy, Spinal _xgenetics |
650 | 0 | 4 |
_aMyotonic Dystrophy _xgenetics |
650 | 0 | 4 | _aTrinucleotide Repeats |
773 | 0 |
_tJournal of inherited metabolic disease _gvol. 20 _gno. 2 _gp. 122-4 |
|
856 | 4 | 0 |
_uhttps://doi.org/10.1023/a:1005388218625 _zAvailable from publisher's website |
999 |
_c9191597 _d9191597 |